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1.
Tetrahedron Lett ; 57(14): p. 1592-1596, 2016.
Article | Sec. Est. Saúde SP, SESSP-IBPROD, Sec. Est. Saúde SP | ID: but-ib13767

ABSTRACT

A general and efficient methodology for the synthesis of novel triazoles has been developed based on a microwave-assisted multicomponent reaction involving alpha-thio aldehyde and propargylamine, with the formation of an imine that in situ reacts with organoazides by copper-catalyzed [3+2] azides-alkyne cycloaddition (CuAAC). The reaction results in a small library of imine 1,4-disubstituted 1,2,3-triazoles. (C) 2016 Elsevier Ltd. All rights reserved.


Subject(s)
Chemistry , Physics
2.
Tetrahedron Lett ; 56(9): p.1153-8, 2015.
Article in English | Sec. Est. Saúde SP, SESSP-IBPROD, Sec. Est. Saúde SP | ID: but-ib11595

Subject(s)
Biochemistry
3.
Tetrahedron Lett ; 55(31): p.4355-8, 2014.
Article in English | Sec. Est. Saúde SP, SESSP-IBPROD, Sec. Est. Saúde SP | ID: but-ib13027

Subject(s)
Biochemistry , Pharmacology
5.
J Org Chem ; 71: p.244-250, 2006.
Article in English | Sec. Est. Saúde SP, SESSP-IBPROD, Sec. Est. Saúde SP | ID: but-ib9115
6.
7.
Tetrahedron Lett ; 39(42): p.7624-, 1998.
Article in English | Sec. Est. Saúde SP, SESSP-IBPROD, Sec. Est. Saúde SP | ID: but-ib11489

Subject(s)
Biochemistry
8.
Tetrahedron Lett ; 38(28): p.4977-80, 1997.
Article in English | Sec. Est. Saúde SP, SESSP-IBPROD, Sec. Est. Saúde SP | ID: but-ib11491
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